Social network you want to login/join with:
Principal Statistical Programmer - Remote, Office or Hybrid - UK, Kingston upon Hull, East Yorkshire
Client: Veramed
Location: Kingston upon Hull, East Yorkshire, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Views: 4
Posted: 26.06.2025
Expiry Date: 10.08.2025
Job Description:
Veramed prides itself on providing high-quality statistics and programming consultancy, along with an industry-leading working environment supporting career growth.
We have an exciting opportunity for a Principal level Statistical Programmer in the UK. We offer home and/or office working, training, support, and a competitive package.
The role involves providing programming support across various projects, clients, and therapeutic areas. The Senior or Principal Programmer may also perform supervisory roles, including line and project management.
Key Responsibilities
The following outlines the scope of the position, which may vary based on business needs.
Technical
* Review clinical trial documents such as protocols, SAPs, CRFs, and CRSs.
* Author, review, and approve study TFL shells and dataset specifications.
* Develop, validate, and document SAS programs for datasets, TFLs, and macros, following good programming practices.
* Identify data issues and outliers.
* Complete, review, and approve CDISC Validation reports.
* Address data and standards issues appropriately.
* Stay informed about emerging standards and their impact on trials.
* Maintain proficiency in SAS and stay updated on developments.
* Ensure study master files and audit-ready documents are maintained.
People Management
* Manage statisticians, programmers, and technical staff, overseeing their performance.
* Coach and mentor staff to achieve excellence.
* Handle onboarding and integration of new staff.
* Provide technical leadership and coaching.
Project Management
* Oversee client projects and portfolios, acting as Project Manager.
* Maintain project plans and proactively manage resources, scope, and risks.
* Ensure project delivery within budget.
* Manage client expectations and resolve issues.
General
* Lead internal and client meetings effectively.
* Present study updates internally and externally.
* Share knowledge within the team and with colleagues.
* Ensure compliance with policies, procedures, and training.
* Build collaborative relationships with internal and client teams.
* Share learnings across projects.
* Develop and deliver internal technical training.
Qualifications:
* BSc, MSc, or PhD in a numerical discipline or relevant industry experience.
* At least 6 years of relevant industry experience.
Additional Requirements
* Understanding of clinical drug development, disease areas, endpoints, and study designs.
What to Expect:
* A supportive and friendly working environment.
* Open-door management policy fostering development.
* A unique CRO approach to managing staff, projects, and relationships.
* Opportunities to own your role and develop skills.
#J-18808-Ljbffr